Virtual Reality Clinical Trial
Official title:
The Effect of Intraoperative Virtual Reality Application on the Level of Anxiety and Vital Findings in Patients Who Will Have Total Knee Replacement Surgery: A Randomized Controlled Study
Verified date | February 2024 |
Source | Bucak State Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Although total knee replacement surgery improves the quality of life of the patients, a significant reduction in knee pain and normalization of the knee joint, the awareness of the surrounding events is a major concern for the patients and negatively affects their vital signs, since most of the patients are awake during the surgery. When the literature is examined, there are no pharmacological methods to reduce anxiety. When distraction techniques are used, patients' anxiety levels are significantly reduced, vital signs are normalized, patient satisfaction is increased and pain is relieved. It has been emphasized that there is a successful method in reducing One of the distraction techniques is the application of virtual reality. This study will be carried out in a randomized controlled experimental design to determine the effect of virtual reality application during surgery on patients who will undergo total knee replacement surgery, on the anxiety level and vital signs of the patients.
Status | Completed |
Enrollment | 70 |
Est. completion date | January 31, 2024 |
Est. primary completion date | April 10, 2023 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Voluntarily agreed to participate in the research - Being 18 years or older - Being able to read and write Turkish - No vision and hearing problems - Not using glasses - Absence of any psychiatric, cognitive or neurological disease Exclusion Criteria: - Patients with visual or hearing impairment - Patients receiving general anesthesia - Those who have previously had total knee replacement surgery |
Country | Name | City | State |
---|---|---|---|
Turkey | Bucak State Hospital | Burdur |
Lead Sponsor | Collaborator |
---|---|
Bucak State Hospital |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | State Anxiety Scale | State Anxiety Scale mean scores of the patients in the intervention and control groups will be compared before and after surgery. A minimum of 20 and a maximum of 80 points can be obtained from the scale. If the scale score approaches 80, it indicates high anxiety. | 10 minute | |
Primary | Respiratory Rate | Just before the start of the operation and every 15 minutes after the operation, the patient's respiratory rate values will be measured on the monitor and the respiratory rate will be recorded in the follow-up form. | 15 minute | |
Primary | Blood Pressure (both systolic and diastolic blood pressure) | Just before the start of the operation and every 15 minutes after the operation, the patient's blood pressure (both systolic and diastolic blood pressure) values will be measured on the monitor and the blood pressure (both systolic and diastolic blood pressure) will be recorded in the follow-up form. | 15 minute | |
Primary | Pulse | Just before the start of the operation and every 15 minutes after the operation, the patient's pulse values will be measured on the monitor and the pulse will be recorded in the follow-up form. | 15 minute | |
Primary | Saturation Value | Just before the start of the operation and every 15 minutes after the operation, the patient's saturation value will be measured on the monitor and the saturation will be recorded in the follow-up form. | 15 minute |
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